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The protein encoded by FGF13 is a member of the fibroblast growth factor (FGF) family. Additionally we are shipping FGF13 Kits (16) and FGF13 Proteins (11) and many more products for this protein.
Showing 10 out of 120 products:
Chicken Polyclonal FGF13 Primary Antibody for WB - ABIN2786194
Popovici, Conchonaud, Birnbaum, Roubin: Functional phylogeny relates LET-756 to fibroblast growth factor 9. in The Journal of biological chemistry 2004
Human Polyclonal FGF13 Primary Antibody for ELISA, WB - ABIN1451931
Ross, Grafham, Coffey, Scherer, McLay, Muzny, Platzer, Howell, Burrows, Bird, Frankish, Lovell, Howe, Ashurst, Fulton, Sudbrak, Wen, Jones, Hurles, Andrews, Scott, Searle, Ramser, Whittaker, Deadman et al.: The DNA sequence of the human X chromosome. ... in Nature 2005
for PCa (show FLVCR1 Antibodies) patients after RP, FGF13 serves as a potential novel prognostic marker that improves prediction of BCR (show BCR Antibodies)-free survival, in particular if combined with other clinical parameters.
The findings of this study reveal a novel cause of this syndrome and underscore the powerful role of FGF13 in control of neuronal excitability.
X-chromosome deletions may be a cause of WS with larger deletions being lethal to males and that FGF13 mutations may be a cause of Wildervanck Syndrome (WS).
Upregulated expression of FGF13/FHF2 mediates resistance to platinum drugs in cervical cancer cells
FGF13 has a role in hair follicle growth and in the hair cycle as shown in a family with X-linked congenital generalized hypertrichosis
FGF13 down-regulated Spry1 (show SPRY1 Antibodies) protein expression, activating the ERK1/2 (show MAPK1/3 Antibodies) pathway by phosphorylation and leading to C2C12 cell differentiation inhibition.
Fibroblast growth factor homologous factors (FGF11 (show FGF11 Antibodies)-14) modulate cardiac calcium channels.
FGF13 has a role in hair follicle growth and in the hair cycle
Genetic deletion of FGF13 in mice results in neuronal migration defects in both the neocortex and the hippocampus. FGF13-deficient mice also exhibit weakened learning and memory.
FGF-13 may play a role in regulating the function of cells in the bulge region and basal layer of the epidermis.
The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked mental retardation mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini.
, fibroblast growth factor 13
, Fibroblast growth factor 13
, fibroblast growth factor homologous factor 2